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Remote Mindfulness-Based Physical Activity Intervention for Postmenopausal Women

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Mayo Clinic

Status

Completed

Conditions

Postmenopausal

Treatments

Behavioral: Mindfulness Audio Recordings

Study type

Interventional

Funder types

Other

Identifiers

NCT05590507
22-007713

Details and patient eligibility

About

The purpose of this study is to figure out if postmenopausal women find a mindfulness audio recording acceptable for use along with physical activity, and to find out if this tool is helpful in increasing daily physical activity.

Enrollment

24 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients self-report as being > 1 year postmenopausal.
  • Patients are able to walk without a walking aid.
  • Patients own and know how to operate a smart phone or tablet.
  • Patients are willing and able to complete the activity monitoring.
  • Patients are self-reportedly underactive.

Exclusion criteria

  • Patients are < 1 year postmenopausal.
  • Patients require a walking aid for daily mobility.
  • Patients do not own a smartphone or table, or are unwilling to use such a device for the purposes of the study.
  • Patients' primary form of exercise is swimming (the activity monitors are not waterproof).
  • Patients are unable or unwilling to complete activity monitoring.
  • Patients are unable to provide informed consent independently.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Group A/Intervention
Experimental group
Description:
Subjects will use mindfulness audio recordings along with their physical activity, and will receive a weekly health coaching phone call along with supplemental educational materials.
Treatment:
Behavioral: Mindfulness Audio Recordings
Group B/Control
No Intervention group
Description:
Subjects will receive education materials on healthy habits for increasing physical activity based on the National Institutes of Health, and bi-weekly check-in phone call.

Trial contacts and locations

1

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Central trial contact

Sey Oloyede

Data sourced from clinicaltrials.gov

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